A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558913



Internal ID20931984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60303327..60304685hg38UCSC Ensembl
chr5:59599154..59600512hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg381359
hg191359
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5768n223
Supporting Variantsnssv18268933
Samples
Known GenesPDE4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558913
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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